Label: SAN SKINLAB CLOTH WET WIPES- benzalkonium chloride 0.13% cloth

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated November 9, 2024

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  • Active Ingredient(s)

    Benzalkonium Chloride 0.13%. Purpose: Antiseptic

  • Purpose

    Antiseptic,

  • Use

    to decrease bacteria on the skin that could cause disease

  • Warnings

    For external use only.

  • WHEN USING

    Keep out of eyes, in case of contact with eyes, flush thoroughly with water, Avoid contact with broken skin, Do Not inhale or ingest

  • STOP USE

    Stop use and ask a doctor if irritation or redness developes condition persist for more than 72 hours.

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

  • Directions

    Wet hands thoroughly with product and allow to dry without wiping

    Not recommended for infants

  • Other information

    • Do not Store above 105F/40 Degree .Do not Freeze
    • Dispose of used wipe in trash, do not flush into toilet
  • Inactive ingredients

    Water ( Aqua) , Alcohol ( Ethanol). Glycerin,Butylene Glycol, Aloe Vera, Citric Acid, 1,2 hexanediol

  • Package Label - Principal Display Panel

    120 wipes120 Wet wipes NDC 75214-120-01

  • INGREDIENTS AND APPEARANCE
    SAN SKINLAB CLOTH WET WIPES 
    benzalkonium chloride 0.13% cloth
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:75214-120
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE0.13 mg  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    ALCOHOL (UNII: 3K9958V90M)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    1,2-HEXANEDIOL (UNII: TR046Y3K1G)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:75214-120-01798 mL in 1 CANISTER; Type 0: Not a Combination Product04/12/2021
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01604/12/2021
    Labeler - HANUL CO.,LTD (557814370)
    Establishment
    NameAddressID/FEIBusiness Operations
    HANUL CO., LTD557814370manufacture(75214-120)
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